ONDANSETRON
- Product NDC
- 51662-1514
- 11-digit product format
- 516621514
- Labeler code
- 51662
- Product ID
- 51662-1514_0f95632b-9d9d-3b6a-e063-6294a90a6bd9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ONDANSETRON
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA090469
- Marketing category
- ANDA
- Marketing start
- 2020-03-31
- Substance
- ONDANSETRON
- Active strength
- 4 mg/1
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4AF302ESOS | ONDANSETRON | 99614-02-5 | ONDANSETRON |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51662-1514-1 | 51662151401 | 2 BLISTER PACK in 1 BAG (51662-1514-1) / 2 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 2 blister pack | 2020-03-31 | No | No | Historical |
| 51662-1514-2 | 51662151402 | 2 BLISTER PACK in 1 BAG (51662-1514-2) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 2 blister pack | 2020-03-31 | No | No | Historical |